Canonical Allele Identifier: CA2680322090

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129516099-A-AATC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516100_129516102dup , CM000668.2:g.129516100_129516102dup	GRCh38
NC_000006.11:g.129837245_129837247dup , CM000668.1:g.129837245_129837247dup	GRCh37
NC_000006.10:g.129878938_129878940dup	NCBI36
NG_008678.1:g.637960_637962dup , LRG_409:g.637960_637962dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-90_1277-88dup	ENSP00000510626.1:n.1277-90_1277-88dup
ENST00000498257.6:c.1277-90_1277-88dup	ENSP00000510533.1:n.1277-90_1277-88dup
ENST00000617695.5:c.9200-90_9200-88dup	ENSP00000481744.2:n.9200-90_9200-88dup
ENST00000618192.5:c.9476-90_9476-88dup	ENSP00000480802.2:n.9476-90_9476-88dup
ENST00000688198.1:n.2190-90_2190-88dup
ENST00000688799.1:c.1277-90_1277-88dup	ENSP00000508458.1:n.1277-90_1277-88dup
ENST00000690858.1:n.4085-90_4085-88dup
ENST00000693461.1:n.1549-90_1549-88dup
ENST00000421865.3:c.9212-90_9212-88dup MANE Select	ENSP00000400365.2:n.9212-90_9212-88dup
ENST00000421865.2:c.9212-90_9212-88dup	ENSP00000400365.2:n.9212-90_9212-88dup
ENST00000617695.4:c.9200-90_9200-88dup	ENSP00000481744.1:n.9200-90_9200-88dup
ENST00000618192.4:c.9209-90_9209-88dup	ENSP00000480802.1:n.9209-90_9209-88dup
NM_000426.3:c.9212-90_9212-88dup , LRG_409t1:c.9212-90_9212-88dup	NP_000417.2:n.9212-90_9212-88dup
NM_001079823.1:c.9200-90_9200-88dup	NP_001073291.1:n.9200-90_9200-88dup
XM_005266981.2:c.9476-90_9476-88dup	XP_005267038.1:n.9476-90_9476-88dup
XM_005266982.2:c.9464-90_9464-88dup	XP_005267039.1:n.9464-90_9464-88dup
XM_011535820.1:c.9470-90_9470-88dup	XP_011534122.1:n.9470-90_9470-88dup
XR_942984.1:n.1460+6375_1460+6377dup
XR_942985.1:n.1324+6375_1324+6377dup
XM_005266981.3:c.9476-90_9476-88dup	XP_005267038.1:n.9476-90_9476-88dup
XM_005266982.3:c.9464-90_9464-88dup	XP_005267039.1:n.9464-90_9464-88dup
XM_011535820.2:c.9470-90_9470-88dup	XP_011534122.1:n.9470-90_9470-88dup
XM_017010851.2:c.9482-90_9482-88dup	XP_016866340.1:n.9482-90_9482-88dup
XM_017010852.1:c.7607-90_7607-88dup	XP_016866341.1:n.7607-90_7607-88dup
XR_001743859.1:n.3900+6375_3900+6377dup
XR_001743860.1:n.1179+6375_1179+6377dup
XR_001743861.1:n.1346+6375_1346+6377dup
XR_001743863.1:n.883-13311_883-13309dup
XR_002956395.1:n.9131+6375_9131+6377dup
XR_002956396.1:n.3126+6375_3126+6377dup
NM_000426.4:c.9212-90_9212-88dup MANE Select	NP_000417.3:n.9212-90_9212-88dup
NM_001079823.2:c.9200-90_9200-88dup	NP_001073291.2:n.9200-90_9200-88dup